Canonical Allele Identifier: CA2673955741
Gene: PART1 HGNC NCBI

Linked Data

gnomAD v4: 5-60529377-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.60529377T>C , CM000667.2:g.60529377T>C GRCh38
NC_000005.9:g.59825204T>C , CM000667.1:g.59825204T>C GRCh37
NC_000005.8:g.59860961T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_024617.1:n.712-27T>C